Genetic resiliency and the Black Death: No apparent loss of mitogenomic diversity due to the Black Death in medieval London and Denmark.


Journal

American journal of physical anthropology
ISSN: 1096-8644
Titre abrégé: Am J Phys Anthropol
Pays: United States
ID NLM: 0400654

Informations de publication

Date de publication:
06 2019
Historique:
received: 22 10 2018
revised: 08 02 2019
accepted: 02 03 2019
pubmed: 10 4 2019
medline: 28 3 2020
entrez: 10 4 2019
Statut: ppublish

Résumé

In the 14th century AD, medieval Europe was severely affected by the Great European Famine as well as repeated bouts of disease, including the Black Death, causing major demographic shifts. This high volatility led to increased mobility and migration due to new labor and economic opportunities, as evidenced by documentary and stable isotope data. This study uses ancient DNA (aDNA) isolated from skeletal remains to examine whether evidence for large-scale population movement can be gleaned from the complete mitochondrial genomes of 264 medieval individuals from England (London) and Denmark. Using a novel library-conserving approach to targeted capture, we recovered 264 full mitochondrial genomes from the petrous portion of the temporal bones and teeth and compared genetic diversity across the medieval period within and between English (London) and Danish populations and with contemporary populations through population pairwise Φ We find no evidence of significant differences in genetic diversity spatially or temporally in our dataset, yet there is a high degree of haplotype diversity in our medieval samples with little exact sequence sharing. The mitochondrial genomes of both medieval Londoners and medieval Danes suggest high mitochondrial diversity before, during and after the Black Death. While our mitochondrial genomic data lack geographically correlated signals, these data could be the result of high, continual female migration before and after the Black Death or may simply indicate a large female effective population size unaffected by the upheaval of the medieval period. Either scenario suggests a genetic resiliency in areas of northwestern medieval Europe.

Identifiants

pubmed: 30964548
doi: 10.1002/ajpa.23820
doi:

Substances chimiques

DNA, Ancient 0
DNA, Mitochondrial 0

Types de publication

Historical Article Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

240-252

Subventions

Organisme : National Health and Medical Research Council (NHMRC)
ID : APP1065106
Pays : International
Organisme : Natural Sciences and Engineering Research Council of Canada (NSERC)
ID : RGPIN-2015-04477
Pays : International
Organisme : Social Sciences and Humanities Research Council of Canada (SSHRC)
ID : 430-2017-01193
Pays : International
Organisme : Social Sciences and Humanities Research Council of Canada (SSHRC)
ID : 435-2018-0465
Pays : International
Organisme : Arbor Biosciences
Pays : International
Organisme : McMaster University
Pays : International
Organisme : Canada Research Chair Program
Pays : International
Organisme : University of Toronto
Pays : International

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Jennifer Klunk (J)

McMaster Ancient DNA Centre, McMaster University, Hamilton, Ontario, Canada.
Department of Biology, McMaster University, Hamilton, Ontario, Canada.

Ana T Duggan (AT)

McMaster Ancient DNA Centre, McMaster University, Hamilton, Ontario, Canada.
Department of Anthropology, McMaster University, Hamilton, Ontario, Canada.

Rebecca Redfern (R)

Center for Human Bioarchaeology, Museum of London, London, UK.

Julia Gamble (J)

Department of Anthropology, University of Manitoba, Winnipeg, Manitoba.

Jesper L Boldsen (JL)

Department of Forensic Medicine, Unit of Anthropology (ADBOU), University of Southern Denmark, Odense, Denmark.

G Brian Golding (GB)

Department of Biology, McMaster University, Hamilton, Ontario, Canada.

Brittany S Walter (BS)

Defense POW/MIA Accounting Agency Laboratory, Offutt AFB, Omaha, Nebraska.

Katherine Eaton (K)

McMaster Ancient DNA Centre, McMaster University, Hamilton, Ontario, Canada.
Department of Anthropology, McMaster University, Hamilton, Ontario, Canada.

Julianna Stangroom (J)

McMaster Ancient DNA Centre, McMaster University, Hamilton, Ontario, Canada.
Department of Anthropology, McMaster University, Hamilton, Ontario, Canada.

Jean-Marie Rouillard (JM)

Arbor Biosciences, Ann Arbor, Michigan.
Department of Chemical Engineering, University of Michigan Ann Arbor, Ann Arbor, Michigan.

Alison Devault (A)

Arbor Biosciences, Ann Arbor, Michigan.

Sharon N DeWitte (SN)

Department of Anthropology, University of South Carolina, Columbia, South Carolina.

Hendrik N Poinar (HN)

McMaster Ancient DNA Centre, McMaster University, Hamilton, Ontario, Canada.
Department of Biology, McMaster University, Hamilton, Ontario, Canada.
Department of Anthropology, McMaster University, Hamilton, Ontario, Canada.
Department of Biochemistry, McMaster University, Hamilton, Ontario, Canada.
Michael G. DeGroote Institute of Infectious Disease Research, McMaster University, Hamilton, Ontario, Canada.

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